A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035039



Internal ID21944382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35468981..35470112hg38UCSC Ensembl
chr15:35761182..35762313hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381132
hg191132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613720
Samples
Known GenesDPH6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035039
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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